Classifications

• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
  • C01F7/00—Compounds of aluminium
  • C01F7/02—Aluminium oxide; Aluminium hydroxide; Aluminates
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
  • A61K8/26—Aluminium; Compounds thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q15/00—Anti-perspirants or body deodorants
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J41/00—Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
  • B01J41/04—Processes using organic exchangers
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
  • C01F7/00—Compounds of aluminium
  • C01F7/48—Halides, with or without other cations besides aluminium
  • C01F7/56—Chlorides
  • C01F7/57—Basic aluminium chlorides, e.g. polyaluminium chlorides

Definitions

• This invention is in the field of materials science and concerns a process for the controlled preparation of hydrolyzed aluminum species, in particular polynuclear Al species, specific examples being the species known as the Al 13 -mer ([Al 13 O 4 (OH) 24 (H 2 O) 12 ] 7+ ) and the Al 30 -mer ([Al 30 O 8 (OH) 56 (H 2 O) 26 ] 18+ ).
• Polynuclear aluminum species are used in a number of materials science applications including the preparation of pillared clays, Al 2 O 3 nanoparticles, antiperspirant actives, catalysts, and composite materials (see Shafran et al, Adv. Eng. Materials, 6(10), 2004, 836, for references to these applications).
• AP actives include basic aluminum chloride species. These have the general formula Al 2 (OH) 6-x Cl x , where x is between about 0.5 and 5. Aluminium chlorohydrate (ACH) is a particular basic aluminum chloride in which x is 5. ACH has been widely used in the AP industry because of its relatively low acidity and subsequent low tendency to cause skin irritation.
• the preparation of the materials involves multiple hydrolysis and condensation reactions, typically resulting in a plethora of species being produced. Whilst the reactions can be difficult to control, it has been identified that some polynuclear Al species are produced and that these are desirable for higher AP efficacy (vide infra).
• ACH actives that are rich in polynuclear Al species, such actives sometimes being called “activated” ACH.
• GB 1,568,831 (Unilever, 1976) describes a route involving heating a solution of ACH under controlled conditions to give polymeric species having a size above 100 Angstroms.
• EP 183,171 B1 (Armour Pharm. Co., 1985) describes a route involving specific heating, drying, and cooling steps, resulting in an ACH having enhanced activity.
• EP 451,395 B1 (Unilever, 1990) describes a process involving the production of ACH having a Band III fraction of at least 20%, the Band III material having particularly good AP efficacy.
• a static ion-exchange process for the preparation of a polynuclear Al species comprising the treatment of an aqueous aluminum chloride solution with a hydroxide-form ion-exchange resin at a temperature from 5° C. to 60° C. for a period of at least 30 minutes.
• the invention enables the preparation of polynuclear Al species in very controlled conditions.
• the invention utilizes a “soft” hydrolysis-condensation process that is in marked contrast to the harsh conditions found in most processes involving reaction with hydroxide ions. This enables good control of the reaction and relatively easy running of the process.
• the invention enables the formation of particularly high levels of preferred polynuclear Al species, such as the Al 13 -mer and, through further reaction, the Al 30 -mer; moreover, this can be done at relatively high Al concentration.
• the invention involves the use of reagents that are widely available and that have low cost: aluminum chloride and an anion exchange resin.
• the reagents are used efficiently and no excess of either reagent is required—this eliminates the need for post-reaction washing and/or other purification of the reaction product.
• the method does not require ‘foreign’ species (e.g. mercury) to be present, a fact that also reduces the need for post-reaction washing and/or other purification.
• the method is simple and produces a high purity product.
• Polynuclear Al species are aluminum species comprising more than one aluminum nucleus.
• the invention is particularly useful in the preparation of the polynuclear Al species having more than two aluminum nuclei, especially those species known as the Al 13 -mer and the Al 30 -mer.
• the method of the invention is used in the preparation of an AP active, in particular a basic aluminum chloride AP active, and especially an ACH AP active, comprising polynuclear Al species.
• an AP active in particular a basic aluminum chloride AP active, and especially an ACH AP active, comprising polynuclear Al species.
• the invention may be used to prepare AP actives having 90% or greater of the aluminum in the form of Al 13 -mer and/or Al 30 -mer.
• polynuclear Al species prepared according to the invention may include species that are complexed with amino acids, such as glycine.
• a key feature of the invention is the use of a hydroxide-form ion-exchange resin. Without wishing to be bound by theory, it is believed that the slow exchange of the hydroxide ion from the resin with chloride ions from solution helps to control the hydrolysis and condensation reactions leading to the production of the polynuclear Al species in high yield.
• a dynamic ion-exchange process is one in which there is physical flow of solution through a bed of ion-exchange resin, the bed typically being in the form of a column. Dynamic ion-exchange tends to lead to concentration perturbations, i.e. uneven concentrations of reactants at different physical locations within the ion-exchange bed. This is an unfavorable situation with regard to the achievement of the benefits of the present invention.
• concentration perturbations i.e. uneven concentrations of reactants at different physical locations within the ion-exchange bed. This is an unfavorable situation with regard to the achievement of the benefits of the present invention.
• the aluminum chloride solution is mixed with the ion-exchange resin and the two are allowed to sit together.
• the ion-exchange resin may be partially or fully in its hydroxide-form; however, the use of an ion-exchange resin that is initially fully in its hydroxide-form is preferred.
• the hydroxide-form ion-exchange resin may be generated from an ion-exchange resin in an alternative form. Often ion exchange resins are bought in a chloride-form and the precursory step involves washing the resin with a hydroxide ion source, such as sodium or potassium hydroxide solution, in order to produce the hydroxide-form ion-exchange resin.
• a hydroxide ion source such as sodium or potassium hydroxide solution
• the mixture of ion-exchange resin and aluminum chloride solution is stirred during the reaction.
• the stirring is preferably done in a manner such that resin retains its integrity, i.e. in a manner such that the resin is not crushed in any way (crushed resin is harder to remove from the solution at the end of the reaction).
• an overhead stirrer made of a corrosion resistant shaft and blade is used.
• High-grade stainless steel is a suitable material for these components
• chemically resistant glass is a preferred material for these components
• Teflon is a particularly preferred material for these components.
• the hydroxide-form ion-exchange resin has a high capacity, in particular a concentration of hydroxide ions of at least 1 mol.kg ⁇ 1 and especially a concentration of hydroxide ions of at least 2 mol.kg ⁇ 1 .
• Such high capacities enable the resin to be kept mobile (i.e. stirred [vide supra]) at high concentrations (mol.dm ⁇ 3 ) of hydroxide ion in the total reaction mixture.
• the ion-exchange resin has a relatively small average bead size. It is preferred that the average bead size (wet) is 75 mesh or less and it is particularly preferred that the average bead size (wet) is 50 mesh or less.
• Having a high concentration of hydroxide ion in the total reaction mixture also enables one to have a high concentration of aluminum chloride in the total reaction mixture, the ratio of one to the other being fixed within relatively narrow bounds, dependent upon the nature of the polynuclear Al species desired (vide infra).
• the concentration of aluminum chloride in the total reaction mixture is typically from 0.05 mol.dm ⁇ 3 to 0.6 mol.dm ⁇ 3 and is preferably from 0.1 mol.dm ⁇ 3 to 0.4 mol.dm ⁇ 3
• the concentration of aluminum chloride in the total reaction mixture may be higher, for example at least 0.4 mol.dm ⁇ 3 and optionally up to 0.6 mol.dm ⁇ 3 .
• the ion-exchange resin used in the present invention is insoluble in water and in the continuous phase of the reaction mixture, i.e. aqueous aluminum chloride solution.
• the ion-exchange resin contains weakly basic, e.g. polyamine, matrix active groups.
• the hydroxide-form ion-exchange resin Prior to mixing with the aluminum chloride solution, it is preferred that the hydroxide-form ion-exchange resin is suspended in water. This allows equilibration of the resin with the aqueous medium, such equilibration being beneficial to the quality of the eventual reaction product.
• the ion-exchange resin may be added to the solution of aluminum chloride or vice versa.
• the solution of aluminum chloride is added to an aqueous suspension of ion-exchange resin.
• a strong acid i.e. an acid having a pK a of less than 2.5
• hydrochloric acid is added to the reaction mixture during the mixing of the aluminum chloride solution with a suspension of the ion-exchange resin. Addition of the acid serves to reduce the pH shock that can occur during this mixing, thereby minimising the production of undesirable components.
• the acid may be added independently of, or as a component of, either the aluminum chloride solution or the suspension of ion-exchange resin or both.
• a strong acid is added to the suspension of ion-exchange resin shortly before this is mixed with the aluminum chloride solution. It is preferred that sufficient acid is added to give the suspension of ion-exchange resin approximately the same pH as the solution of aluminum chloride with which it is to be mixed. It is particularly preferred that the suspension of ion-exchange resin and the aluminum chloride solution have a pH within 1 unit of each other when they are mixed. In this embodiment, it is important that the mixing is performed quickly, preferably being completed within two minutes and more preferably within one minute of the completion of the acidification of the suspension of ion-exchange resin.
• H hydrolysis ratio
• the hydrolysis ratio:H is the ratio of hydroxide ion equivalents to aluminum ion equivalents in the reaction mixture, this ratio being termed the hydrolysis ratio:H.
• H is preferably from 2.1 to 2.6, more preferably from 2.3 to 2.5, and most preferably from 2.4 to 2.5.
• Al 13 -mer H is most preferably about 2.45, while for generation of the Al 30 -mer, H is most preferably about 2.40.
• the source of the hydroxide ions is solely the hydroxide-form ion-exchange resin.
• the source of the aluminum ions is solely the aluminum chloride solution.
• the pH of the reaction mixture increases during the course of the preparation, especially during the early stages.
• the initial pH is typically below 3.5 and, to optimise production of polynuclear Al species, it is preferred that the pH is kept below 4.75 throughout the course of the preparation.
• the rate of increase of the reaction pH preferably decreases during the course of the reaction. It is particularly preferred that d(pH)/dt does not increase during any period of the preparation. It is especially preferred that d(pH)/dt has reduced to less than 0.015 within 30 minutes of the aluminum chloride solution and ion-exchange resin being mixed, pH being conventional units ( ⁇ log 10 [H + ]), and time t being expressed in minutes.
• the preparation is preferably carried out at a temperature of from 18° C. to 40° C., more preferably at from 20° C. to 35° C., and most preferably at from 20° C. to 30° C.
• Lower temperatures are not desirable because they tend to slow the reaction down.
• Higher temperatures are not desirable because they tend to lead to a lower quality product, having greater inhomogeneity and/or a lower level of polynuclear Al species.
• the time during which the aluminum chloride solution and ion-exchange resin are in contact is preferably at least 45 minutes, more preferably at least 1 hour, and most preferably at least 2 hours. Shorter reaction times are undesirable because the reaction may not have reached the optimum extent of completion. For economic reasons and/or product quality reasons, it is preferred that the reaction time is not too great.
• the reaction time is preferably less than 6 hours, more preferably less than 4 hours, and most preferably less than 3 hours.
• the optimum reaction temperature and time are related, shorter reaction times being required at higher temperatures and vice versa.
• the reaction is carried out at from 10° C. to 25° C. for 2 to 4 hours, whilst in other embodiments it may be preferred that the reaction is carried out at from 25° C. to 40° C. for 30 minutes to 2 hours.
• the resin is removed from the solution, typically by filtration.
• a small amount of further hydroxide-form ion-exchange resin typically from 0.1% to 0.5% of the weight of resin initially used
• This further reaction is preferably performed at ambient temperature for a period of from 1 day to 1 week.
• the amount of further ion-exchange resin to be added may be calculated from an analysis of a portion of the solution of polynuclear species produced during the initial reaction.
• washing the ion-exchange resin with a source of hydroxide ion is used as a means of regenerating the hydroxide form of the resin after it has been used in accordance with the invention.
• a source of hydroxide ion such as aqueous sodium or potassium hydroxide solution
• the aqueous aluminum chloride solution is treated with the hydroxide-form ion-exchange resin
• the ion-exchange resin is then separated from the resulting solution of polynuclear Al species, regenerated by treatment with a source of hydroxide ions, and then re-used to prepare further polynuclear Al species.
• This recycling of the ion-exchange resin adds to the efficiency and environmental acceptability of the manufacturing process.
• the ion-exchange resin is washed with hydrochloric acid, typically of concentration about 10% w/v, prior to being washed with a source of hydroxide ion.
• the acid wash serves to remove residual aluminum species from the resin and thereby improve the performance of the regenerated resin.
• Preparation of the Al 30 -mer polynuclear species requires ageing of the solution of polynuclear species prepared according to the first aspect of the invention, following removal of the ion-exchange resin.
• the solution of polynuclear species prepared according to the first aspect of the invention may be aged at from 60 to 95° C., preferably at from 70 to 90° C., and more preferably at from 80 to 85° C.
• the ageing is preferably performed for from 12 to 72 hours, more preferably from 24 to 64 hours, and most preferably from 24 and 36 hours. In general, the longer the ageing time, the more complete is the transformation of lower species into the Al 30 -mer species.
• a process of preparation analogous to that described in the first aspect of the invention may be used to prepare aluminum hydroxide sols of surprisingly narrow particle size distribution. Such materials may be advantageous in the ceramics field and in chromatographic applications.
• the analogous process comprises the treatment of an aqueous aluminum salt solution with a hydroxide-form ion-exchange resin at a temperature from 5° C. to 60° C. for a period of at least 30 minutes, H being chosen to be greater than 2.6, preferably greater than 2.7, and more preferably greater than 2.8.
• the aluminum salt employed is preferably chloride, but may be nitrate or some other water-soluble salt. Following removal of the ion-exchange resin by filtration, a colloidal dispersion or sol of aluminum hydroxide remains.
• this sol may be aged, preferable at 60° C. or less and preferably for one month or less, in order to produce an aluminum hydroxide sol of selected particle size.
• the longer the ageing period employed the greater is the particle size of the aluminum hydroxide colloidal dispersions produced.
• Higher ageing temperature also leads to larger particle sizes. Nano-sized colloidal dispersions of selected particle size may be produced in this manner.
• the solution of aluminum species remaining after removal of the ion-exchange resin may be dried to give a solid sample of polynuclear Al species in powder form. This may be done on an industrial scale by freeze-drying or spray-drying. Freeze-drying is generally considered to be a less harsh technique and may be preferred for this reason. Spray drying tends to result in a dried salt with a more consistent and desirable particle size distribution and may be preferred for this reason.
• the dried powder be cooled as soon as possible after the drying step, for example by conveying it from the drying stage to the next stage (e.g. a storage stage) in a cooled, low humidity current of air.
• the procedure is performed to give a water content of the resulting (dried) AP active of preferably no lower than about 2%, more preferably at least about 4%, even more preferably at least 6%, and most preferably at least 8% by weight of the active. It is not desirable to dry to particularly low water levels, because the drying regimes to which the active needs to be subjected to get to such water levels may be deleterious to the quality of the active resulting, in particular its content of desirable polynuclear species, such as the Al 13 -mer.
• the drying procedure is performed to give a water content of the resulting (dried) AP active of preferably less than 12% and more preferably less than 10% by weight of the active. It is believed that reducing the water content of the active is desirable for its long-term stability.
• Water content may conveniently be measured using a moisture balance, for example a Sartorius MA30 moisture balance, used on an “auto” programme with a set point of 100° C.
• a moisture balance for example a Sartorius MA30 moisture balance, used on an “auto” programme with a set point of 100° C.
• a commercially available anion exchange resin (Amberlite IRA67, 50 mesh (wet), ex Sigma) was washed using deionized distilled water and was transformed into the hydroxide-form using 2M potassium hydroxide solution prior to a second extensive washing with water and drying for 48 hours under ambient conditions.
• the titre of the resin was established using an excess of 1M hydrochloric acid solution and back-titration with a standard volumetric solution potassium hydrogen carbonate.
• hydroxide-form ion-exchange resin Various amounts of the hydroxide-form ion-exchange resin were suspended in 80 ml aliquots of deionized water. To these suspensions were added 20 ml aliquots of 1M aluminum chloride solution and the mixtures were stirred at 25 ⁇ 0.2° C. in a Pyrex glass reactor for 3 hours. After this time, the resin was removed by filtration through a 70 micron HDPE Buchner filter funnel to leave an aqueous solution of aluminum species as the final product.
• H being the ratio of hydroxide ion equivalents to aluminum ion equivalents in the reaction mixture. H values from 0.5 to 3.0 were investigated.
• H The effect of H upon the level of aluminum species in the final product is shown in Table 1. From these figures, it may be seen that levels of H from 2.1 to 2.6 all produce high levels of Al 13 -mer, with H values of from 2.4 to 2.5 being particularly preferred for this purpose. It is noteworthy that aluminum hydroxide becomes the dominant species present at higher H values.
• Quantitative 27 Al solution NMR was used to determine the amounts of mono- and bi-nuclear species present and the amount of Al 13 -mer present.
• the amount of aluminum hydroxide was calculated as the difference between the sum of these amounts and the amount of aluminum in the starting solutions (0.2 M), as described in the work of Deschaume et al, Adv. Eng. Materials, 6(10), 2004, 836.
• a portion of 1M aluminum chloride solution containing 0.25 M hydrochloric acid was added rapidly to a stirred suspension of ion-exchange resin in 0.1 M hydrochloric acid, the time between acidification of the ion-exchange resin and addition of the acidified aluminum chloride solution being kept to a minimum.
• the amounts of reagents were selected to give an H value of 2.40 and a final aluminum concentration of 0.4 M. After equilibration had been achieved (approximately 3 hours), the resin was removed by filtration and the solution of aluminum species was heated at 85° C. for 38 hours. Analysis of the resulting solution revealed that greater than 90% of the aluminum was present as the Al 30 -mer.
• One part was stored at room temperature for 48 hours and produced a near mono-disperse aluminum hydroxide sol of mean particle size 35 nm, as determined by DLS.
• the other part was stored at 60° C. for 48 hours and produced a near mono-disperse aluminum hydroxide sol of mean particle size 80 nm, as determined by DLS.

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• 2006
  • 2006-03-22 AT AT06723918T patent/ATE431318T1/de not_active IP Right Cessation
  • 2006-03-22 ES ES06723918T patent/ES2323980T3/es not_active Expired - Lifetime
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  • 2006-03-22 PL PL06723918T patent/PL1863741T3/pl unknown
  • 2006-03-22 WO PCT/EP2006/002958 patent/WO2006103092A1/en not_active Ceased
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  • 2006-03-22 DE DE602006006812T patent/DE602006006812D1/de not_active Expired - Lifetime
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